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Coral Reefs

, Volume 36, Issue 4, pp 1245–1252 | Cite as

Assessing the utility of eDNA as a tool to survey reef-fish communities in the Red Sea

  • Joseph D. DiBattistaEmail author
  • Darren J. Coker
  • Tane H. Sinclair-Taylor
  • Michael Stat
  • Michael L. Berumen
  • Michael Bunce
Note
First Online:

Abstract

Relatively small volumes of water may contain sufficient environmental DNA (eDNA) to detect target aquatic organisms via genetic sequencing. We therefore assessed the utility of eDNA to document the diversity of coral reef fishes in the central Red Sea. DNA from seawater samples was extracted, amplified using fish-specific 16S mitochondrial DNA primers, and sequenced using a metabarcoding workflow. DNA sequences were assigned to taxa using available genetic repositories or custom genetic databases generated from reference fishes. Our approach revealed a diversity of conspicuous, cryptobenthic, and commercially relevant reef fish at the genus level, with select genera in the family Labridae over-represented. Our approach, however, failed to capture a significant fraction of the fish fauna known to inhabit the Red Sea, which we attribute to limited spatial sampling, amplification stochasticity, and an apparent lack of sequencing depth. Given an increase in fish species descriptions, completeness of taxonomic checklists, and improvement in species-level assignment with custom genetic databases as shown here, we suggest that the Red Sea region may be ideal for further testing of the eDNA approach.

Keywords

Biodiversity Coral reef Environmental DNA Metabarcoding Next-generation sequencing 
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Notes

Acknowledgements

This study was funded by KAUST Award No. CRG-1-2012-BER-002 and baseline research funds to M.L.B., as well as a Curtin University Early Career Research Fellowship to J.D.D., M.S., and M.B. acknowledge the support of ARC Linkage Project (LP160100839) to explore marine metabarcoding applications. The authors would also like to acknowledge KAUST’s Coastal and Marine Resources Core Lab for logistical support, as well as Matthew Power, Megan Coghlan, and Brendan Chapman for DNA sequencing assistance.

Supplementary material

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Supplementary material 1 (DOCX 388 kb)
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Supplementary material 2 (DOCX 105 kb)
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Supplementary material 3 (DOCX 13 kb)
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Supplementary material 4 (FASTA 1533 kb)

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Copyright information

© Springer-Verlag GmbH Germany 2017

Authors and Affiliations

  1. 1.Trace and Environmental DNA Laboratory, Department of Environment and AgricultureCurtin UniversityPerthAustralia
  2. 2.Division of Biological and Environmental Sciences and EngineeringKing Abdullah University of Science and TechnologyThuwalSaudi Arabia

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